The company strictly implements the Drug Administration Law, Vaccine Administration Law, Drug Production Quality Management Standards, Drug Business Quality Management Standards, Vaccine Storage and Transportation Management Standards and other laws and regulations, and has formulated strict standardized management procedures for the entire life cycle of drugs.

The company has established a continuous improvement of the quality management system, since the establishment of the company has accepted more than 30 domestic regulatory authorities GMP, GVP, GSP inspection, nearly 10 foreign regulatory authorities inspection, including the international certification organization PIC/S certification.

In the new era and new situation, Chengda Biology will continue to implement various laws and regulations on drug production, take the initiative to assume the main responsibility of drug production enterprises, earnestly fulfill the obligations of quality management throughout the life cycle of vaccines, and continuously improve the quality management system. improve the ability of risk prevention, ensure the quality of drug production, effectively ensure the safety of drug use by the public, and better serve the society.